Clinical Research Associate
On-siteTel Aviv, Tel Aviv, Israel or Kfar Saba, Central District, Israel
Job Summary
Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard Operating Procedures, GCP and ICH guidelines, and applicable regulatory requirements. Perform all required monitoring activities at study sites to ensure subject safety, data integrity, and quality. Verify the protection of study participants through informed consent procedures and protocol compliance. Review CRFs and subject source documentation for validity, completeness, and accuracy. Verify proper management and accountability of Investigational Product. Prepare timely monitoring visit reports, document findings and follow-up actions, update required tracking systems, and escalate issues as appropriate. Ensure site documentation is maintained appropriately, support eTMF and ISF compliance, and update CTMS and other required project systems with accurate site information.
Required Qualifications
- Bachelor's Degree, preferably in Life Sciences, Nursing, or equivalent
- Minimum 1 year of relevant clinical research experience or relevant academic background related to clinical trials or clinical development activities
- Understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements
- Strong written and verbal communication skills with fluency in English
- Excellent organizational skills and ability to work independently as well as within a matrix team environment
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